Thrombocytes 6

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	48951-9003	48951-9003-1	I	Inactivated by FDA		2026-10-12

Adverse event summaries are temporarily unavailable. Other product information remains available.

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-9003-1	Thrombocytes 6	10 in 1 BOX	LIQUID	10		3
48951-9003-1	Thrombocytes 6	1 mL in 1 AMPULE	LIQUID	1		3

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
EQUUS CABALLUS WHOLE	ACTIVE INGREDIENT	R7AD7Y06PL	THROMBOCYTES 6 LIQUID [URIEL PHARMACY INC.]	1
EQUUS CABALLUS WHOLE	ACTIVE MOIETY	R7AD7Y06PL	THROMBOCYTES 6 LIQUID [URIEL PHARMACY INC.]	1
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	THROMBOCYTES 6 LIQUID [URIEL PHARMACY INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	THROMBOCYTES 6 LIQUID [URIEL PHARMACY INC.]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-9003	THROMBOCYTES 6 LIQUID [URIEL PHARMACY INC.]	3	Legacy NDC, 2 package rows	20180524_b9a90acd-0e58-4e65-959e-18b989cffe96.zip

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
R7AD7Y06PL	EQUUS CABALLUS WHOLE	EQUUS CABALLUS WHOLE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-9003-1	48951900301	10 AMPULE in 1 BOX (48951-9003-1) > 1 mL in 1 AMPULE	10 ampule	2009-09-01	0000-00-00	No	No	Current